Incidental Mutation 'R4374:Cd209c'
ID 325035
Institutional Source Beutler Lab
Gene Symbol Cd209c
Ensembl Gene ENSMUSG00000040165
Gene Name CD209c antigen
Synonyms mSIGNR2, SIGNR2
MMRRC Submission 041118-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.120) question?
Stock # R4374 (G1)
Quality Score 225
Status Validated
Chromosome 8
Chromosomal Location 3990222-4004746 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to C at 4004635 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold Q91ZW9
Predicted Effect noncoding transcript
Transcript: ENSMUST00000127592
SMART Domains Protein: ENSMUSP00000120433
Gene: ENSMUSG00000040165

DomainStartEndE-ValueType
transmembrane domain 51 73 N/A INTRINSIC
Meta Mutation Damage Score 0.1807 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.8%
Validation Efficiency 97% (38/39)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd2 A G 7: 78,973,278 (GRCm39) M86V probably benign Het
Acin1 C A 14: 54,891,351 (GRCm39) probably benign Het
Aebp2 T A 6: 140,599,984 (GRCm39) probably benign Het
Akap13 A G 7: 75,258,732 (GRCm39) E452G probably damaging Het
Amz1 T C 5: 140,738,194 (GRCm39) S184P possibly damaging Het
Armh4 T A 14: 50,007,893 (GRCm39) T527S probably damaging Het
Ccdc83 A T 7: 89,875,986 (GRCm39) L295* probably null Het
Cpsf7 A T 19: 10,517,001 (GRCm39) I368F probably damaging Het
Csf1r G A 18: 61,252,078 (GRCm39) C520Y probably damaging Het
Dapk1 A G 13: 60,867,498 (GRCm39) D235G probably benign Het
Ercc1 G A 7: 19,081,057 (GRCm39) probably benign Het
Fktn T C 4: 53,720,201 (GRCm39) S72P probably damaging Het
Frem2 C A 3: 53,452,923 (GRCm39) V2189F possibly damaging Het
Gm10845 G T 14: 80,100,563 (GRCm39) noncoding transcript Het
Hk1 C A 10: 62,151,319 (GRCm39) K10N probably damaging Het
Lama1 A G 17: 68,111,513 (GRCm39) M2255V probably benign Het
Lrsam1 G T 2: 32,845,203 (GRCm39) T104K possibly damaging Het
Myh6 T A 14: 55,199,565 (GRCm39) I249F probably damaging Het
Myo7a G A 7: 97,751,881 (GRCm39) T54M probably damaging Het
Or52ae7 T C 7: 103,119,278 (GRCm39) S11P probably damaging Het
Or5k15 A C 16: 58,710,242 (GRCm39) C114G probably benign Het
Osbpl8 T A 10: 111,105,280 (GRCm39) I245N possibly damaging Het
Pfkp A G 13: 6,671,025 (GRCm39) S135P probably damaging Het
Phf20l1 C T 15: 66,476,686 (GRCm39) T260I possibly damaging Het
Pole T A 5: 110,485,071 (GRCm39) I395K possibly damaging Het
Ppp6r2 T G 15: 89,149,361 (GRCm39) C216W probably damaging Het
Pramel7 C T 2: 87,320,415 (GRCm39) A293T probably benign Het
Rpl11 G A 4: 135,778,454 (GRCm39) probably benign Het
Scamp3 G A 3: 89,089,234 (GRCm39) probably null Het
Setbp1 T C 18: 78,903,137 (GRCm39) R177G probably damaging Het
Sh2b3 G T 5: 121,966,549 (GRCm39) probably benign Het
Tbc1d30 A G 10: 121,130,617 (GRCm39) F271S probably damaging Het
Tpo T C 12: 30,153,151 (GRCm39) E401G possibly damaging Het
Zdhhc13 T C 7: 48,458,589 (GRCm39) Y308H probably damaging Het
Zfp112 C T 7: 23,825,798 (GRCm39) H589Y probably damaging Het
Zmiz1 T C 14: 25,636,434 (GRCm39) S140P probably damaging Het
Other mutations in Cd209c
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00089:Cd209c APN 8 3,990,339 (GRCm39) missense probably damaging 1.00
IGL01340:Cd209c APN 8 3,995,892 (GRCm39) missense probably benign 0.00
IGL02682:Cd209c APN 8 3,990,324 (GRCm39) missense probably damaging 0.99
R1311:Cd209c UTSW 8 3,995,908 (GRCm39) start codon destroyed probably benign
R1859:Cd209c UTSW 8 3,994,953 (GRCm39) missense probably benign
R4375:Cd209c UTSW 8 4,004,635 (GRCm39) exon noncoding transcript
R4377:Cd209c UTSW 8 4,004,635 (GRCm39) exon noncoding transcript
R4769:Cd209c UTSW 8 3,994,953 (GRCm39) missense probably benign
R4786:Cd209c UTSW 8 3,995,698 (GRCm39) missense possibly damaging 0.77
R4841:Cd209c UTSW 8 3,995,905 (GRCm39) missense probably benign 0.00
R4842:Cd209c UTSW 8 3,995,905 (GRCm39) missense probably benign 0.00
R4869:Cd209c UTSW 8 3,994,077 (GRCm39) missense probably benign 0.00
R5333:Cd209c UTSW 8 3,994,976 (GRCm39) missense probably damaging 1.00
R5835:Cd209c UTSW 8 3,995,699 (GRCm39) missense probably benign 0.01
R6369:Cd209c UTSW 8 3,994,984 (GRCm39) missense probably damaging 1.00
R6497:Cd209c UTSW 8 3,994,122 (GRCm39) missense possibly damaging 0.72
R6591:Cd209c UTSW 8 3,995,680 (GRCm39) missense probably benign 0.14
R6691:Cd209c UTSW 8 3,995,680 (GRCm39) missense probably benign 0.14
R7181:Cd209c UTSW 8 3,995,712 (GRCm39) missense probably benign 0.01
R8067:Cd209c UTSW 8 3,995,700 (GRCm39) missense probably benign 0.12
R8701:Cd209c UTSW 8 3,995,892 (GRCm39) missense probably benign 0.00
R9722:Cd209c UTSW 8 3,995,905 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- AAGGAGTATCTGGTGCCACTG -3'
(R):5'- GAGCCATTACATGCTCATCCATTC -3'

Sequencing Primer
(F):5'- ATCTGGTGCCACTGGGTATC -3'
(R):5'- ATCCATTCCAGGAATGCTGG -3'
Posted On 2015-07-06